具有层内 π-π 相互作用的自剥离双金属金属有机框架层,可实现高效电气传输和二氧化碳电还原

IF 9.6 1区 化学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Xiaohui Yao, Dongxu Cui, Changyan Zhu, Jingting He, Fanfei Meng, Shuai Yang, Man Dong, Guogang Shan*, Min Zhang, Chunyi Sun*, Xinlong Wang and Zhongmin Su, 
{"title":"具有层内 π-π 相互作用的自剥离双金属金属有机框架层,可实现高效电气传输和二氧化碳电还原","authors":"Xiaohui Yao,&nbsp;Dongxu Cui,&nbsp;Changyan Zhu,&nbsp;Jingting He,&nbsp;Fanfei Meng,&nbsp;Shuai Yang,&nbsp;Man Dong,&nbsp;Guogang Shan*,&nbsp;Min Zhang,&nbsp;Chunyi Sun*,&nbsp;Xinlong Wang and Zhongmin Su,&nbsp;","doi":"10.1021/acsmaterialslett.4c0090210.1021/acsmaterialslett.4c00902","DOIUrl":null,"url":null,"abstract":"<p >Two-dimensional metal–organic frameworks (2D MOF) have attracted great attention in the electrocatalytic reduction of CO<sub>2</sub> owing to their well-defined structure and high surface area. Nevertheless, how to combine accessible metal active sites with high electron transfer still poses challenges in structural assembly. Herein, two-dimensional AgCe-MOFs with intralayer π–π stacking interactions were assembled by linking one-dimensional Ce–O chains to Ag(I). Its nanosheet can be facilely prepared via self-exfoliation upon the loss of uncoordinated interlayer acetonitrile. The 2D AgCe-MOF nanosheets’ merits of more exposed active sites and efficient electron transfer channels have displayed outstanding electrochemical performance and 99.5% selectivity in electrocatalytic CO<sub>2</sub> reduction to CO. The establishment of efficient electrical transport channels and high exposure of catalytic sites in a framework through designed supramolecular interactions is expected to be a potential strategy for the construction of efficient electrocatalysts.</p>","PeriodicalId":19,"journal":{"name":"ACS Materials Letters","volume":"6 11","pages":"5112–5119 5112–5119"},"PeriodicalIF":9.6000,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-exfoliating Bimetallic Metal–Organic Framework Layer with Intralayer π–π Interactions for Efficient Electrical Transport and CO2 Electroreduction\",\"authors\":\"Xiaohui Yao,&nbsp;Dongxu Cui,&nbsp;Changyan Zhu,&nbsp;Jingting He,&nbsp;Fanfei Meng,&nbsp;Shuai Yang,&nbsp;Man Dong,&nbsp;Guogang Shan*,&nbsp;Min Zhang,&nbsp;Chunyi Sun*,&nbsp;Xinlong Wang and Zhongmin Su,&nbsp;\",\"doi\":\"10.1021/acsmaterialslett.4c0090210.1021/acsmaterialslett.4c00902\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Two-dimensional metal–organic frameworks (2D MOF) have attracted great attention in the electrocatalytic reduction of CO<sub>2</sub> owing to their well-defined structure and high surface area. Nevertheless, how to combine accessible metal active sites with high electron transfer still poses challenges in structural assembly. Herein, two-dimensional AgCe-MOFs with intralayer π–π stacking interactions were assembled by linking one-dimensional Ce–O chains to Ag(I). Its nanosheet can be facilely prepared via self-exfoliation upon the loss of uncoordinated interlayer acetonitrile. The 2D AgCe-MOF nanosheets’ merits of more exposed active sites and efficient electron transfer channels have displayed outstanding electrochemical performance and 99.5% selectivity in electrocatalytic CO<sub>2</sub> reduction to CO. The establishment of efficient electrical transport channels and high exposure of catalytic sites in a framework through designed supramolecular interactions is expected to be a potential strategy for the construction of efficient electrocatalysts.</p>\",\"PeriodicalId\":19,\"journal\":{\"name\":\"ACS Materials Letters\",\"volume\":\"6 11\",\"pages\":\"5112–5119 5112–5119\"},\"PeriodicalIF\":9.6000,\"publicationDate\":\"2024-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Materials Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsmaterialslett.4c00902\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Materials Letters","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsmaterialslett.4c00902","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

二维金属有机框架(2D MOF)因其明确的结构和高比表面积而在二氧化碳的电催化还原中备受关注。然而,如何将易接近的金属活性位点与高电子传递结合起来,仍然是结构组装中的难题。本文通过将一维 Ce-O 链与 Ag(I) 连接,组装出具有层内 π-π 堆垛相互作用的二维 AgCe-MOF。在失去非配位层间乙腈后,通过自剥离可以方便地制备其纳米片。二维 AgCe-MOF 纳米片具有更多暴露的活性位点和高效电子传递通道的优点,在电催化 CO2 还原成 CO 的过程中表现出卓越的电化学性能和 99.5% 的选择性。通过设计超分子相互作用在框架中建立高效电子传输通道和高暴露催化位点有望成为构建高效电催化剂的一种潜在策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Self-exfoliating Bimetallic Metal–Organic Framework Layer with Intralayer π–π Interactions for Efficient Electrical Transport and CO2 Electroreduction

Self-exfoliating Bimetallic Metal–Organic Framework Layer with Intralayer π–π Interactions for Efficient Electrical Transport and CO2 Electroreduction

Two-dimensional metal–organic frameworks (2D MOF) have attracted great attention in the electrocatalytic reduction of CO2 owing to their well-defined structure and high surface area. Nevertheless, how to combine accessible metal active sites with high electron transfer still poses challenges in structural assembly. Herein, two-dimensional AgCe-MOFs with intralayer π–π stacking interactions were assembled by linking one-dimensional Ce–O chains to Ag(I). Its nanosheet can be facilely prepared via self-exfoliation upon the loss of uncoordinated interlayer acetonitrile. The 2D AgCe-MOF nanosheets’ merits of more exposed active sites and efficient electron transfer channels have displayed outstanding electrochemical performance and 99.5% selectivity in electrocatalytic CO2 reduction to CO. The establishment of efficient electrical transport channels and high exposure of catalytic sites in a framework through designed supramolecular interactions is expected to be a potential strategy for the construction of efficient electrocatalysts.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Materials Letters
ACS Materials Letters MATERIALS SCIENCE, MULTIDISCIPLINARY-
CiteScore
14.60
自引率
3.50%
发文量
261
期刊介绍: ACS Materials Letters is a journal that publishes high-quality and urgent papers at the forefront of fundamental and applied research in the field of materials science. It aims to bridge the gap between materials and other disciplines such as chemistry, engineering, and biology. The journal encourages multidisciplinary and innovative research that addresses global challenges. Papers submitted to ACS Materials Letters should clearly demonstrate the need for rapid disclosure of key results. The journal is interested in various areas including the design, synthesis, characterization, and evaluation of emerging materials, understanding the relationships between structure, property, and performance, as well as developing materials for applications in energy, environment, biomedical, electronics, and catalysis. The journal has a 2-year impact factor of 11.4 and is dedicated to publishing transformative materials research with fast processing times. The editors and staff of ACS Materials Letters actively participate in major scientific conferences and engage closely with readers and authors. The journal also maintains an active presence on social media to provide authors with greater visibility.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信